Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia-Reference-Cited by-同舟云学术

Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia

Published:2013-07-07 Issue:8 Volume:45 Page:937-941
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Sakaguchi Hirotoshi,Okuno Yusuke,Muramatsu Hideki,Yoshida Kenichi,Shiraishi Yuichi,Takahashi Mariko,Kon Ayana,Sanada Masashi,Chiba Kenichi,Tanaka Hiroko,Makishima Hideki,Wang Xinan,Xu Yinyan,Doisaki Sayoko,Hama Asahito,Nakanishi Koji,Takahashi Yoshiyuki,Yoshida Nao,Maciejewski Jaroslaw P,Miyano Satoru,Ogawa Seishi,Kojima Seiji

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2698.pdf

Reference40 articles.

1. Pinkel, D. et al. Differentiating juvenile myelomonocytic leukemia from infectious disease. Blood 91, 365–367 (1998).

2. Loh, M.L. et al. Mutations in CBL occur frequently in juvenile myelomonocytic leukemia. Blood 114, 1859–1863 (2009).

3. Muramatsu, H. et al. Mutations of an E3 ubiquitin ligase c-Cbl but not TET2 mutations are pathogenic in juvenile myelomonocytic leukemia. Blood 115, 1969–1975 (2010).

4. Pérez, B. et al. Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia. Br. J. Haematol. 151, 460–468 (2010).

5. Ng, S.B. et al. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat. Genet. 42, 790–793 (2010).

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